A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593226



Internal ID20966297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73508225..73508709hg38UCSC Ensembl
chr10:75267983..75268467hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226413
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593226
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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